# K962769: Horizon Hip System

- Pathway: 510(k) (Traditional)
- Applicant: Biologically Oriented Prostheses
- Decided: Oct 3, 1996 after 79 days
- Product code: LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented)
- Device class: 2
- Regulation: 21 CFR 888.3358
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Depuy AML femoral stems: named in the summary without a submission number
- (no number) AML Plus Depuy cup: named in the summary without a submission number
- (no number) Depuy AML system: named in the summary without a submission number

## Most influential descendants
- K971681: SMC Femoral Hip Component (1997), 1 descendant of its own
- K990821: Providence Cup System (1999), 0 descendants of its own
- K981302: SMC 28MM Ceramic Femoral Heads (1998), 0 descendants of its own

## Indications for use
Both systems are indicated for treatment of osteoarthritis, rheumatoid arthritis, avascular necrosis, and traumatic arthritis.

Source page: https://510kreport.com/device/K962769
Methodology: https://510kreport.com/methodology